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(E)-(4R,5R-3-ISOPROPYL-4-METHYL-5-PHENYL-1,3,2-OXAZABOROLIDYL)-(4-CHLOROPHENYL)-ETHENE

Compound with spectra: 2 NMR

(E)-(4R,5R-3-ISOPROPYL-4-METHYL-5-PHENYL-1,3,2-OXAZABOROLIDYL)-(4-CHLOROPHENYL)-ETHENE
SpectraBase Compound ID AUQuDImRfBQ
InChI InChI=1S/C20H23BClNO/c1-15(2)23-16(3)20(18-7-5-4-6-8-18)24-21(23)14-13-17-9-11-19(22)12-10-17/h4-16,20H,1-3H3/b14-13+/t16-,20+/m1/s1
InChIKey DCKWEPWCCYQFBK-AKUXXTROSA-N
Mol Weight 339.7 g/mol
Molecular Formula C20H23BClNO
Exact Mass 339.156122 g/mol
Enantiomer InChIKey DCKWEPWCCYQFBK-OUNRHQKTSA-N

View Spectrum of (E)-(4R,5R-3-ISOPROPYL-4-METHYL-5-PHENYL-1,3,2-OXAZABOROLIDYL)-(4-CHLOROPHENYL)-ETHENE

11B NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6

View Spectrum of (E)-(4R,5R-3-ISOPROPYL-4-METHYL-5-PHENYL-1,3,2-OXAZABOROLIDYL)-(4-CHLOROPHENYL)-ETHENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
3-butyl-2-(4-chlorophenyl)-5-(4-(trimethylsilyloxy)phenyl)-1,3,2-oxazaborolidine
3-butyl-2-(4-fluorophenyl)-5-(4-(trimethylsilyloxy)phenyl)-1,3,2-oxazaborolidine
3-butyl-2-phenyl-5-(4-(trimethylsilyloxy)phenyl)-1,3,2-oxazaborolidine
(+)-N-(1-Phenylethyl)-N-(2-phenyloxetan-3-yl)acetamide
3,4-dimethyl-5-phenyl-2,2-bis(trideuteriomethyl)oxazolidine
3,7-bis[2'-(t-Butyldimethylsilyloxy)-1'-methyl-2'-phenylethyl]-3,7-diazabicyclo[3.3.1]nonan-9-one
(2-R/S,3-R/S)-N-PHENYLMETHYL-(2-TRIMETHYLSILYL)-N-(2-PHENYLOXETAN-3-YL)-CARBAMATE
(2R,4S,5R)-2-[4-(DIMETHYLAMINO)-PHENYL]-3,4-DIMETHYL-5-DIPHENYL-OXAZOLIDINE
(2S,4S,5R)-2-[4-(DIMETHYLAMINO)-PHENYL]-3,4-DIMETHYL-5-DIPHENYL-OXAZOLIDINE
2-[Acetyl(methyl)amino]-1-phenylpropyl cyclohexyl(methyl)phosphinate
Title Journal or Book Year
Vinylborane Formation in Rhodium-Catalyzed Hydroboration of Vinylarenes. Mechanism versus Borane Structure and Relationship to Silation Journal of the American Chemical Society 1994

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